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TASC SOPS

The TASC Clinical Research Guidelines Committee have approved a library of Standard Operating Procedures (SOPs) for TASC and research staff to follow to ensure that clinical research is conducted and reported in compliance with the principles of Good Clinical Practice (GCP), regulatory requirements and the Research Governance Framework.

Clinical Trials of Investigational Medicinal Products (CTIMPs) sponsored or co-sponsored by the University of Dundee and/or NHS Tayside must be conducted in accordance with the TASC SOPs agreed upon at risk assessment.

TASC will send email notifications (Hot Tips) to researchers when existing SOPs are updated or new SOPs are released. 

Please refer to the TASC website frequently to ensure that you are always working to the current SOP versions.

Click HERE  for the index of TASC SOPs (Tab 1) and Associated Documents. (Tab 2)

 

TASC SOPs have been grouped into 5 sections.  Please click on the relevant section to find your SOP of choice:

 

Data Management & Statistics SOPs

Quality Assurance SOPs

Research Governance SOPs

Safety & Pharmacovigilance SOPs

Trial Management SOPS

 

TASC Policies

The TASC Research Governance Committee is responsible for the oversight of TASC Policies.

TASC will send email notifications (Hot Tips) to researchers when existing SOPs are updated or new SOPs are released.

Click on TASC Policies to view the current versions.

 For queries or comments regarding TASC SOPs or policies, please contact Dr Valerie Godfrey, TASC QA Manager, v.godfrey@dundee.ac.uk

 TASC Policies

© University of Dundee and NHS Tayside Health Board, 2018

TASC do not permit the copying of SOPs contents and logos without reference to source of ownership.